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Akt (pSer473) ELISA Data, Cat. No CBA005
Akt (pSer473) from extracts of Jurkat cells cultured in RPMI + 10% FCS were serially diluted in standard diluent buffer. The optical density of each dilution was plotted against the Akt (pSer473) standard curve. The data indicates that the standard accurately reflects full length Akt (pSer473) content from Jurkat samples.

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AKT ELISA Specificity
The specificity of this assay for Akt phosphorylated at serine 473 was confirmed by peptide competition. The data presented in figure 2 shows that only the phosphopeptide containing the phosphorylated serine could block the ELISA signal. The same sequence containing non-phosphorylated serine at position 473 did not block the signal. The assay was found to have no cross-reactivity with the following recombinant phosphoproteins tested at 100 ng/ml: p38 MAPK, p44 ERK1, p42 ERK2, JNK1, human insulin receptor, rat insulin receptor, and human HGFR (cmet).

 
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